Conner M K, Cheng M, Biegel J A
Mutat Res. 1984 Mar;126(1):35-46. doi: 10.1016/0027-5107(84)90167-2.
A path probability model is described for evaluation of sister-chromatid exchanges (SCEs) induced by alkylating agents following treatment of G1 cells at the beginning of the first or second cycles of BrdUrd incorporation, or during G1 corresponding to an exact cell-cycle interval preceding BrdUrd incorporation. Algebraic expressions are derived for calculations of expected induced SCE frequencies (over baseline levels) in second and third (reciprocal and nonreciprocal SCEs) division cells for the described treatment protocols. The derivations take into consideration: p, the probability of a specific lesion inducing an SCE; rn, the extent of repair within the nth post-treatment cycle; and X, the number of lesions induced. Expressions are also derived for expected ratios of single: twin exchanges in endoreduplicated or tetraploid cells.
描述了一种路径概率模型,用于评估在第一个或第二个BrdUrd掺入周期开始时对G1期细胞进行处理后,或在与BrdUrd掺入之前精确的细胞周期间隔相对应的G1期期间,由烷化剂诱导的姐妹染色单体交换(SCE)。针对所描述的处理方案,推导了代数表达式,用于计算第二代和第三代(相互和非相互SCE)分裂细胞中预期的诱导SCE频率(超过基线水平)。推导过程考虑了:p,特定损伤诱导SCE的概率;rn,处理后第n个周期内的修复程度;以及X,诱导的损伤数量。还推导了内复制或四倍体细胞中单交换与双交换预期比率的表达式。